Linked Data
MyVariant Identifiers:
chrX:g.63412219C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64192339C>A , CM000685.2:g.64192339C>A | GRCh38 |
| NC_000023.10:g.63412219C>A , CM000685.1:g.63412219C>A | GRCh37 |
| NC_000023.9:g.63328944C>A | NCBI36 |
| NG_021345.1:g.18406G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374869.8:c.948G>T MANE Select | ENSP00000364003.4:p.Val316= | |
| ENST00000330258.3:c.948G>T | ENSP00000329117.3:p.Val316= | |
| ENST00000374869.7:c.948G>T | ENSP00000364003.3:p.Val316= | |
| NM_152424.3:c.948G>T | NP_689637.3:p.Val316= | |
| XM_011530858.1:c.948G>T | XP_011529160.1:p.Val316= | |
| NM_152424.4:c.948G>T MANE Select | NP_689637.3:p.Val316= |